Living Data Technologies Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K033657 | MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V | December 19, 2003 |
| K023701 | ANGIONEW-IV | January 30, 2003 |